Label: CHILDRENS IBUPROFEN- ibuprofen suspension

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated October 26, 2018

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    100 mg/5 mL 200 mg/10 mL

    For Hospital Use Only

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient (in each 5 mL = 1 teaspoonful)

    Ibuprofen 100 mg (NSAID)1


    1
    nonsteroidal anti-inflammatory drug
  • Purposes

    Pain reliever/Fever reducer

  • Uses

    temporarily:

    relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache
    reduces fever
    This product is intended for use in children.
  • Warnings

    Allergy alert

    Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:

    hives
    facial swelling
    blisters
    asthma (wheezing)
    shock
    skin reddening
    rash

    If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning

    This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if your child:

    has had stomach ulcers or bleeding problems
    takes a blood thinning (anticoagulant) or steroid drug
    takes other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
    takes more or for a longer time than directed

    Sore throat warning

    Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by doctor.

    Do not use

    if the child has ever had an allergic reaction to any other pain reliever/fever reducer
    right before or after heart surgery

    Ask a doctor before use if

    stomach bleeding warning applies to your child
    child has a history of stomach problems, such as heartburn
    child has problems or serious side effects from taking pain relievers or fever reducers
    child has not been drinking fluids
    child has lost a lot of fluid due to vomiting or diarrhea
    child has high blood pressure, heart disease, liver cirrhosis, or kidney disease
    child has asthma
    child is taking a diuretic

    Ask a doctor or pharmacist before use if the child is

    under a doctor's care for any serious condition
    taking any other drug

    When using this product

    give with food or milk if stomach upset occurs
    the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

    Stop use and ask a doctor if

    child experiences any of the following signs of stomach bleeding:
    feels faint
    vomits blood
    has bloody or black stools
    has stomach pain that does not get better
    the child does not get any relief within first day (24 hours) of treatment
    fever or pain gets worse or lasts more than 3 days
    redness or swelling is present in the painful area
    any new symptoms appear

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

  • Directions

    use as directed per healthcare professional
    this product does not contain directions or complete warnings for adult use
    do not give more than directed
    shake cups well before using
    if needed, repeat dose every 6 - 8 hours
    do not use more than 4 times a day
  • Other Information

    each teaspoon contains: sodium 2 mg
    store at 20-25°C (68-77°F)
    do not freeze
    See individual label or shipper label for lot number and expiration date.
  • Inactive Ingredients

    anhydrous citric acid, artificial mixed berry flavor, D&C yellow #10, FD&C red #40, glycerin, high fructose corn syrup, hypromellose, polysorbate 80, purified water, sodium benzoate, sorbitol solution, xanthan gum

  • SPL UNCLASSIFIED SECTION

    Alcohol Free, Gluten Free

  • How Supplied

    Available :

    Overbagged with 5 cups (10 mL per unit dose cup) per bag, NDC 55154-1585-5

  • SPL UNCLASSIFIED SECTION

    Manufactured By:
    Perrigo Company
    515 Eastern Avenue
    Allegan, MI 49010

    Packaged By:
    Precision Dose, Inc.
    722 Progressive Lane
    S. Beloit, IL 61080

    Distributed by:

    Cardinal Health

    Dublin, OH 43017

    L49748610318

    LI 587
    Rev. 04/13

  • Principal Display Panel

    Children’s Ibuprofen Oral Suspension

    200 mg/ 10 mL

    5 x 10 mL Unit Dose Cups

    bag label
  • INGREDIENTS AND APPEARANCE
    CHILDRENS IBUPROFEN 
    ibuprofen suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-1585(NDC:68094-503)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Ibuprofen (UNII: WK2XYI10QM) (Ibuprofen - UNII:WK2XYI10QM) Ibuprofen200 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    anhydrous citric acid (UNII: XF417D3PSL)  
    D&C yellow NO. 10 (UNII: 35SW5USQ3G)  
    FD&C red NO. 40 (UNII: WZB9127XOA)  
    glycerin (UNII: PDC6A3C0OX)  
    high fructose corn syrup (UNII: XY6UN3QB6S)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    polysorbate 80 (UNII: 6OZP39ZG8H)  
    water (UNII: 059QF0KO0R)  
    sodium benzoate (UNII: OJ245FE5EU)  
    sorbitol (UNII: 506T60A25R)  
    xanthan gum (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorORANGEScore    
    ShapeSize
    FlavorBERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55154-1585-510 in 1 BAG09/14/2006
    110 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07493709/14/2006
    Labeler - Cardinal Health (603638201)